BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
The Senior Director of CMO and Distribution Logistics, Clinical Supply Chain is responsible for overseeing the Clinical Supply Chain vision and strategy providing leadership over the DP Supply Planning, CMO operation and Distribution management. Ensures organization effectively manages vendor relationships and activities and acts as point of escalation for CMOs performance issues for both operational execution and distribution. The position provides leadership, manages direct reports as well as mentors team members as required to ensure optimal performance. Represents DP Planning, CMO management and Distribution & Logistics on the Global Clinical Supply Chain Leadership Team and ensures strategic alignment to Global Clinical Supply Chain and BeiGene’s strategic goals. Builds strong relationships with BeiGene functional leadership (including but not limited to clinical Operation, Quality, Regulatory, CMC, and GRDS) to ensure alignment of organizations and prompt resolution of critical issues.
Has an expert working knowledge of supply chain best practices and experience working within a cGMP and GCP environment. Has strong cross-cultural awareness and communication skills to lead in a fast paced, multi- cultural company.
Essential Functions of the job:
- Interface with internal manufacturing sites and external CMO/vendors on related activities for DP/FG and distribution operations, providing robust solutions and implementation actions.
- Oversee the management of production schedules to maximize supply efficiency, minimize waste while identifying risk and developing mitigation plans by working with supply chain leaders and CMC project managers.
- Act as point of escalation if deliverables and timelines are jeopardized, communicating to appropriate internal and external stakeholders as needed.
- Participate in CMO Site visits as requested.
- Ensure team supports QA and Legal in establishing QA and MSA agreements with all CMO’s and assuring that Product Specific Requirements (PSR’s) are established before projects are initiated.
- Participate in Compliance group’s audit process from planning through implementation, result evaluation, and CMO response review.
- Support inspection readiness activities as required. Drive the close out of audit commitments and CAPA’S as appropriate.
- Oversee distribution and logistics teams for storage, Import & Export, distribution, drug return, destruction, and Depot Management.
- Accountable for ensuring successful delivery of DP and FG delivery to depots and clinical sites.
- Develop and maintain relationship with global Courier/broker vendors.
- Oversee the development of the Import permit application strategy globally.
- Ensure site/CMO/vendor metrics, key issues, production status, operational performance summary updates are tracked and reported by implementing KPIs.
- Participate and lead process/performance improvement initiatives with cross functionally with stakeholders contributing to global/regional initiatives or programs.
- Lead monthly Supply Review Meeting of CD&OP and present/report supply planning performance and related discussions.
- Build strategic relationships with internal functional groups and ensure alignment.
- Oversee the annual forecast and budgeting target vs. actual for CMO management /DP planning and distribution activities.
- Responsible ensuring team supports investigation of exceptions to determine root causes, implement CAPAs and drive closure.
- Ensure robust systems and processes are in place to enable execution of operational and logistical tasks in a cGMP compliant manner.
- Collaborate and author department policies and procedures.
Supervisory Responsibilities:
- Lead Supply packaging team , CMO and distribution management team. in global locations including US, EU, and China for BeiGene. Manage direct reports as well as provide mentoring to their teams as required.
Competencies:
- Experience working in a global, complex supply chain organization within the biopharma industry.
- Experience leading multi-disciplinary department(s) and building up the team
- Strong ability to collaborate and build strategic relationships with internal (Clinical Operations, Quality, CMC, Regulatory, etc.) stakeholders.
- Demonstrates advanced knowledge of global clinical trials and the drug development process.
- Experience in vendor oversight and managing external partnerships and relations.
- Experience with biologics and small molecule supply chain.
- Understands comprehensive global pharmaceutical regulatory requirements (e.g. cGMP, ICH/GDP, GCP, 21 CFR Part 11, and Annex 13).
- Experience in deviation investigation and CAPA implementation.
- Ability to work effectively in cross-functional and multi-cultural teams.
Education Required:
Bachelor or Master Degree in Science or Business Administration, Operations Management, or similar education required, Supply Chain Management, and/or Management of Science or equivalent filed is preferred.
Packaging experience is beneficial (small molecule, biologic devices).
Experience with Device Manufacturing, DeviceAssembly, and process validation is a plus
12+ years’ progressive experience
5+ years of people leadership and development experience
Computer Skills:
Proficient in Microsoft Office applications, Planning applications and models, IRT/IXRS systems, MRP/ERP systems
Other Qualifications:
Due to global nature of company early morning or evening meetings may be required
Travel: 30%
BeiGene Global Competencies
When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
- Fosters Teamwork
- Provides and Solicits Honest and Actionable Feedback
- Self-Awareness
- Acts Inclusively
- Demonstrates Initiative
- Entrepreneurial Mindset
- Continuous Learning
- Embraces Change
- Results-Oriented
- Analytical Thinking/Data Analysis
- Financial Excellence
- Communicates with Clarity
Salary Range: $183,300.00 - $253,300.00 annually
BeiGene is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeiGene Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer and we value diversity. BeiGene does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.
